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Fanconi- Bickel Syndrome: mutation in an Indian patient.
Ekbote AV, Mandal K, Agarwal I, Sinha R, Danda S. Ekbote AV, et al. Among authors: mandal k. Indian J Pediatr. 2012 Jun;79(6):810-2. doi: 10.1007/s12098-011-0568-9. Epub 2011 Oct 5. Indian J Pediatr. 2012. PMID: 21972075
Smith-Magenis Syndrome: Face Speaks.
Gupta R, Gupta N, Nampoothiri S, Mandal K, Kishore Y, Sharma P, Kabra M, Phadke SR. Gupta R, et al. Among authors: mandal k. Indian J Pediatr. 2016 Jun;83(6):589-93. doi: 10.1007/s12098-015-1940-y. Epub 2015 Dec 17. Indian J Pediatr. 2016. PMID: 26676648
Fanconi-Bickel Syndrome: Another Novel Mutation in SLC2A2.
Amita M, Srivastava P, Mandal K, De S, Phadke SR. Amita M, et al. Among authors: mandal k. Indian J Pediatr. 2017 Mar;84(3):236-237. doi: 10.1007/s12098-016-2236-6. Epub 2016 Oct 14. Indian J Pediatr. 2017. PMID: 27738794 No abstract available.
Hotspots in PTPN11 Gene Among Indian Children With Noonan Syndrome.
Narayanan DL, Pandey H, Moirangthem A, Mandal K, Gupta R, Puri RD, Patil SJ, Phadke SR. Narayanan DL, et al. Among authors: mandal k. Indian Pediatr. 2017 Aug 15;54(8):638-643. doi: 10.1007/s13312-017-1125-z. Epub 2017 Jun 4. Indian Pediatr. 2017. PMID: 28607217 Free article.
752 results